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一种新型的甲状腺激素受体异源二聚化伴侣。过氧化物酶体增殖物激活受体。

A novel heterodimerization partner for thyroid hormone receptor. Peroxisome proliferator-activated receptor.

作者信息

Bogazzi F, Hudson L D, Nikodem V M

机构信息

Genetics and Biochemistry Branch, NIDDK, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Biol Chem. 1994 Apr 22;269(16):11683-6.

PMID:8163464
Abstract

Retinoid-like receptors play a central role in hormonal responses by forming heterodimers with other nuclear hormone receptors. In this study we have identified the peroxisome proliferator-activated receptor (PPAR) as a new thyroid hormone receptor (THR) auxiliary nuclear protein, heterodimerizing with THR in solution. Although these heterodimers do not recognize a classical thyroid hormone response element (TRE) characterized by direct repeat separated by four nucleotides (DR+4), PPAR behaves as a dominant negative regulator of thyroid hormone (TH) action. However, a TH-dependent positive effect is elicited by selective interaction of the THR beta-PPAR but not the THR alpha-PPAR heterodimer with a novel TRE (DR+2). The critical region of THR beta was mapped to 3 amino acids in the distal box of the DNA binding domain. Hence, PPAR can positively or negatively influence TH action depending on TRE structure and THR isotype.

摘要

类视黄醇受体通过与其他核激素受体形成异源二聚体,在激素反应中发挥核心作用。在本研究中,我们已确定过氧化物酶体增殖物激活受体(PPAR)是一种新的甲状腺激素受体(THR)辅助核蛋白,它在溶液中与THR形成异源二聚体。尽管这些异源二聚体不识别由四个核苷酸分隔的直接重复序列(DR+4)所表征的经典甲状腺激素反应元件(TRE),但PPAR表现为甲状腺激素(TH)作用的显性负调节因子。然而,THRβ-PPAR而非THRα-PPAR异源二聚体与新型TRE(DR+2)的选择性相互作用引发了TH依赖性的正向效应。THRβ的关键区域定位于DNA结合结构域远端盒中的3个氨基酸。因此,PPAR可根据TRE结构和THR亚型对TH作用产生正向或负向影响。

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